This is a 6 episode collection of personal interviews with someone who has Cystic Fibrosis and had a lung transplant. The intended audience is broad and may include someone who has CF, is a parent of a child with CF, is a child of someone with CF, has had or may need a transplant or anyone who would love to be inspired by a story of optimism!
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This is a 6 episode collection of personal interviews with someone who has Cystic Fibrosis and had a lung transplant. The intended audience is broad and may include someone who has CF, is a parent of a child with CF, is a child of someone with CF, has had or may need a transplant or anyone who would love to be inspired by a story of optimism!
In our 6th and final episode, Bern explores new challenges that come after being a transplant recipient. Her incredible gratitude for life shines through and is contagious. Thank you for listening. We hope you may consider donating to Cystic Fibrosis research and talk with your family about the impact of being an organ donor.
Air of Optimism
This is a 6 episode collection of personal interviews with someone who has Cystic Fibrosis and had a lung transplant. The intended audience is broad and may include someone who has CF, is a parent of a child with CF, is a child of someone with CF, has had or may need a transplant or anyone who would love to be inspired by a story of optimism!
